Müller C, Kowenz-Leutz E, Grieser-Ade S, Graf T, Leutz A
Max-Delbrück-Centrum für Molekulaire Medizin, Berlin, Germany.
EMBO J. 1995 Dec 15;14(24):6127-35. doi: 10.1002/j.1460-2075.1995.tb00303.x.
CAAT/enhancer binding proteins (C/EBPs) are transcriptional activators implicated in the differentiation processes of various cell lineages. We have shown earlier that NF-M, the chicken homolog of C/EBP beta, is specifically expressed in myelomonocytic and eosinophilic cells of the hematopoietic system. To investigate the role of NF-M in hematopoietic cell lineage commitment, we constructed a conditional form of the protein by fusing it to the hormone binding domain of the human estrogen receptor. This construct was stably expressed in a multipotent progenitor cell line transformed by the Myb-Ets oncoprotein. We report here that both NF-M-dependent promoter constructs and resident genes could be activated by addition of beta-estradiol to the NF-M-estrogen receptor expressing progenitors. At the same time, we observed a down-regulation of progenitor-specific surface markers and the up-regulation of differentiation markers restricted to the eosinophil and myeloid lineages. In addition to the onset of differentiation, cell death was induced with typical apoptotic features. Our results suggest that NF-M plays an important role in commitment along the eosinophil lineage and in the induction of apoptosis.
CAAT/增强子结合蛋白(C/EBPs)是参与多种细胞谱系分化过程的转录激活因子。我们之前已经表明,C/EBPβ的鸡同源物NF-M在造血系统的髓单核细胞和嗜酸性细胞中特异性表达。为了研究NF-M在造血细胞谱系定向分化中的作用,我们通过将其与人雌激素受体的激素结合域融合构建了一种条件形式的该蛋白。该构建体在由Myb-Ets癌蛋白转化的多能祖细胞系中稳定表达。我们在此报告,通过向表达NF-M-雌激素受体的祖细胞中添加β-雌二醇,NF-M依赖的启动子构建体和驻留基因均可被激活。同时,我们观察到祖细胞特异性表面标志物下调,而仅限于嗜酸性粒细胞和髓系谱系的分化标志物上调。除了分化开始外,还诱导了具有典型凋亡特征的细胞死亡。我们的结果表明,NF-M在嗜酸性粒细胞谱系的定向分化和凋亡诱导中起重要作用。